Multiple carboxylase deficiency
|Multiple carboxylase deficiency|
|Classification and external resources|
Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.
If left untreated, the symptoms can include feeding problems, hypotonia, generalised erythematous rash with skin exfoliation and alopecia, failure to thrive, seizure, coma, developmental delay, foul smelling urine, metabolic acidosis, ketosis and hyperammonemia.
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